Physiologically relevant and portable tandem ubiquitin-binding domain stabilizes polyubiquitylated proteins.

ABSTRACT: Ubiquitylation of proteins can be a signal for a variety of cellular processes beyond the classical role in proteolysis. The different signaling functions of ubiquitylation are thought to rely on ubiquitin-binding domains (UBDs). Several distinct UBD families are known, but their functions are not understood in detail, and mechanisms for interpretation and transmission of the ubiquitin signals remain to be discovered. One interesting example of the complexity of ubiquitin signaling is the Saccharomyces cerevisiae transcription factor Met4, which is regulated by a single lysine-48 linked polyubiquitin chain that can directly repress activity of Met4 or induce degradation by the proteasome. Here we show that ubiquitin signaling in Met4 is controlled by its tandem UBD regions, consisting of a

SUBMITTER: Tyrrell A 

PROVIDER: S-EPMC2993400 | biostudies-literature | 2010 Nov

REPOSITORIES: biostudies-literature